GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **5901 - 5925** of **9988** in total

« First

‹ Prev

…

233

234

235

236

237

238

239

240

241

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
3631	inositol polyphosphate-4-phosphatase type I A	INPP4A Type I inositol 3,4-bisphosphate 4-phosphatase	Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma autosomal dominant dyskeratosis congenita 1 bladder carcinoma cancer early myoclonic encephalopathy embryoma intrinsic asthma lung cancer lung non-small cell carcinoma pancreatic cancer pancreatic carcinoma situs inversus tuberous sclerosis urinary bladder cancer
3628	inositol polyphosphate-1-phosphatase	INPP1	bipolar disorder cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer obsolete major affective disorder 2
54891	INO80 complex subunit D	INO80D
54617	INO80 complex ATPase subunit	INO80 INO80 complex subunit A INO80A KIAA1259 hINO80
83729	inhibin subunit beta E	INHBE
3626	inhibin subunit beta C	INHBC
3625	inhibin subunit beta B	INHBB
3624	inhibin subunit beta A	INHBA
3623	inhibin subunit alpha	INHA
54556	inhibitor of growth family member 3	ING3
64423	inverted formin 2	INF2
3619	inner centromere protein	INCENP
55765	innate immunity activator	INAVA
9118	internexin neuronal intermediate filament protein alpha	INA
50939	interphotoreceptor matrix proteoglycan 2	IMPG2
3617	interphotoreceptor matrix proteoglycan 1	IMPG1
3615	inosine monophosphate dehydrogenase 2	IMPDH2
3613	inositol monophosphatase 2	IMPA2 myo-inositol monophosphatase 2	bipolar disorder borderline personality disorder cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma depressive disorder dysthymic disorder embryoma endometriosis of ovary endometriosis of uterus endometriosis intermittent explosive disorder major depressive disorder melancholic depression mood disorder neurotic disorder nonpapillary renal cell carcinoma obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
3612	inositol monophosphatase 1	IMPA1 myo-inositol monophosphatase 1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive intellectual developmental disorder 59 autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
10989	inner membrane mitochondrial protein	IMMT
10994	ilvB acetolactate synthase like	ILVBL
64771	inflammation and lipid regulator with UBA-like and NBR1-like domains	ILRUN
3609	interleukin enhancer binding factor 3	ILF3
3608	interleukin enhancer binding factor 2	ILF2
286676	immunoglobulin like domain containing receptor 1	ILDR1

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements